Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K123149 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general ... | 2 | 10/09/2020 |
FEI # 3025504317 Getinge Group Logistics America, LLC |
| Servo-I ventilator system CO2 analyzer. Part number 65 23 588. | 2 | 02/27/2015 |
FEI # 3008355164 Maquet Cardiovascular Us Sales, Llc |
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